OBO ID: DOID:0110931
Term Name: nemaline myopathy 10 Search Ontology:
Synonyms:
  • congenital myopathy 10
  • NEM10
Definition: A nemaline myopathy characterized by early-onset generalized muscle weakness and hypotonia with respiratory insufficiency and feeding difficulties that has_material_basis_in homozygous or compound heterozygous mutation in the LMOD3 gene on chromosome 3p14. https://www.ncbi.nlm.nih.gov/pubmed/25250574
References:
Ontology: Human Disease   ( DOID:0110931 )
Relationships
is a type of:
OTHER nemaline myopathy 10 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
LMOD3 Nemaline myopathy 10 616165
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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